7-Bromo-4-methyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione
95%
- Product Code: 50279
CAS:
78756-36-2
| Molecular Weight: | 269.09 g./mol | Molecular Formula: | C₁₀H₉BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06015648 | |
| Melting Point: | Boiling Point: | 480.7±45.0 °C | |
| Density: | 1.580±0.06 g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of benzodiazepine derivatives, which are widely known for their applications in treating anxiety, insomnia, and other central nervous system disorders. Researchers often modify its core structure to enhance bioactivity, optimize pharmacokinetic properties, or reduce potential side effects. Additionally, it is employed in organic synthesis to create complex heterocyclic compounds, which are further explored for their potential therapeutic effects in drug discovery programs. Its bromine substituent also makes it a versatile building block for cross-coupling reactions, enabling the construction of diverse chemical libraries for biological screening.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,304.00 |
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| 0.250 | 10-20 days | ฿18,900.00 |
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| 1.000 | 10-20 days | ฿36,288.00 |
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7-Bromo-4-methyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of benzodiazepine derivatives, which are widely known for their applications in treating anxiety, insomnia, and other central nervous system disorders. Researchers often modify its core structure to enhance bioactivity, optimize pharmacokinetic properties, or reduce potential side effects. Additionally, it is employed in organic synthesis to create complex heterocyclic compounds, which are further explored for their potential therapeutic effects in drug discovery programs. Its bromine substituent also makes it a versatile building block for cross-coupling reactions, enabling the construction of diverse chemical libraries for biological screening.
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